NCT03254914
Completed
Not Applicable
A Multi-center, Cluster-randomized, Prospective, Observational Study
ConditionsHypertension
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Hypertension
- Sponsor
- Boryung Pharmaceutical Co., Ltd
- Enrollment
- 3554
- Locations
- 1
- Primary Endpoint
- Rate of reaching target blood pressure
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
The purpose of this study is to evaluate the effect of home blood pressure monitoring on controlling blood pressure and correlation between home blood pressure and clinic blood pressure in hypertensive patients receiving two or more concomitant antihypertensive agents including fimasartan
Detailed Description
A multi-center, cluster-randomized, prospective, observational study
Investigators
Eligibility Criteria
Inclusion Criteria
- •Subjects who voluntarily signed informed consent for participating in this clinical study
- •Male and female over the age of 19
- •Hypertensive patients receiving two or more concomitant anti-hypertensive agents including fimasartan
Exclusion Criteria
- •Renal dialysis patients.
- •Diabetic nephropathy patients taking angiotensin-converting enzyme inhibitor.
- •Severe renal disorder
- •Subjects with hereditary disorders of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption.
- •Medical history with hypersensitivity to Fimasartan
- •Pregnant women or lactating female.
- •Participate in another clinical trial.
Outcomes
Primary Outcomes
Rate of reaching target blood pressure
Time Frame: 12 weeks after treatment
Rate of reaching target blood pressure after treatment for 12 weeks
Study Sites (1)
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